1 |
(Vogelmeier et al., 2011) |
455 |
Tiotropium |
Moderate-to-very-severe COPD |
In patients with moderate-to-very-severe COPD, tiotropium is more effective than salmeterol in preventing exacerbations |
2 |
(Wedzicha et al., 2013) |
364 |
QVA149 |
COPD stages III-IV, and one or more moderate COPD exacerbation in the past year |
The dual bronchodilator QVA149 was superior in preventing moderate to severe COPD exacerbations compared with glycopyrronium, with concomitant improvements in lung function and health status |
3 |
(Vogelmeier et al., 2013) |
238 |
QVA149 |
COPD stages II-III, without exacerbations in the previous year |
Once-daily QVA149 provides significant, sustained, and clinically meaningful improvements in lung function versus twice-daily salmeterol-fluticasone, with significant symptomatic benefit |
4 |
(Vestbo et al., 2016) |
231 |
Corticosteroid, fluticasone furoate, and vilanterol |
Moderate COPD and heightened cardiovascular risk |
In patients with moderate COPD and heightened cardiovascular risk, treatment with fluticasone furoate and vilanterol did not affect mortality or cardiovascular outcomes, reduced exacerbations, and was well tolerated |
5 |
(Singh et al., 2016) |
216 |
Single-inhaler combination of an extra fine formulation of beclometasone dipropionate, formoterol fumarate, and glycopyrronium bromide (BDP/FF/GB) |
COPD had post-bronchodilator FEV1 of lower than 50%, one or more moderate-to-severe COPD exacerbation in the previous 12 months, CAT ≥10, and a Baseline Dyspnea Index focal score of 10 or less |
This paper provide evidence for the clinical benefits of stepping up patients with COPD from an inhaled corticosteroid/long-acting β2-agonist combination treatment to triple therapy using a single inhaler |
6 |
(Izquierdo et al., 2021) |
13 |
Clinical Management of COPD in a Real-World Setting |
COPD |
This study identifies the main features of an unselected COPD population and the major errors made in the management of the disease |